US8241485B2ExpiredUtilityA1
Biosensor electrode mediators for regeneration of cofactors
Est. expiryOct 16, 2017(expired)· nominal 20-yr term from priority
C12Q 1/005Y10T29/49155C12Q 1/006G01N 27/3272C12Q 1/004
71
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Cited by
43
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18
Claims
Abstract
The present invention is based on the discovery of NAD + and NADP + mediator compounds that do not bind irreversibly to thiol groups in the active sites of intracellular dehydrogenase enzymes. Such mediator compounds avoid a common mode of enzyme inhibition. The mediators can therefore increase the stability and reliability of the electrical response in amperometric electrodes constructed from NAD- or NADP-dependent enzymes.
Claims
exact text as granted — not AI-modified1. A method of determining concentration of an analyte in a sample, the method comprising:
applying the sample to a biosensor, wherein the biosensor comprises:
at least two substrates;
a plurality of electrodes comprising a fill indicator electrode, a working electrode, and a reference or counter/reference electrode; and
at least one reaction zone comprising an enzyme, a cofactor, and a mediator associated with at least the working electrode, wherein the mediator consists of one of the two following formulae:
where X and Y can independently be oxygen, sulphur, CR 3 R 4 , NR 3 , or NR 3 R 4+ or the functional group CZ 1 Z 2 , where Z 1 and Z 2 are electron withdrawing groups; R 1 and R 2 can independently be a substituted or unsubstituted aromatic or heteroaromatic group; and R 3 and R 4 can independently be a hydrogen atom, a hydroxyl group or a substituted or unsubstituted alkyl, aryl, heteroaryl, amino, alkoxyl, or aryloxyl group;
applying a potential between the working electrode and the reference/counter electrode within 3 seconds of the sample covering the plurality of electrodes; and
measuring a current between the working electrode and the reference/counter electrode to determine the concentration of the analyte in the sample.
2. The method according to claim 1 , wherein the method comprises applying the potential between the working electrode and the reference/counter electrode as soon as the sample covers the plurality of electrodes.
3. The method according to claim 1 , wherein the method comprises applying a potential that is 200 mV or less.
4. The method according to claim 3 , wherein measuring the current between the working electrode and the counter/reference electrode comprises measuring a signal that increases linearly with the concentration of the analyte in the sample.
5. The method according to claim 1 , wherein determining the concentration of the analyte in the sample comprises measuring the current between the working electrode and the reference/counter electrode for about 5 to 60 seconds.
6. The method according to claim 1 , wherein the mediator is 1,10-phenanthroline quinone.
7. The method according to claim 1 , wherein the enzyme is glucose dehydrogenase or 3-hydroxybutyrate dehydrogenase.
8. The method according to claim 1 , wherein one of the at least two substrates is a spacer.
9. The method according to claim 1 , wherein at least a portion of the plurality of electrodes are positioned in the reaction zone.
10. The method according to claim 1 , wherein the electrodes comprise carbon.
11. The method according to claim 1 , wherein the biosensor comprises a strip-type identifier.
12. The method according to claim 11 , wherein the strip-type identifier comprises a barcode.
13. The method according to claim 11 , wherein the strip-type identifier comprises a magnetic strip.
14. The method according to claim 11 , wherein the strip-type identifier comprises a notch.
15. The method according to claim 11 , wherein the strip-type identifier comprises an optical detector.
16. The method according to claim 11 , wherein the strip-type identifier comprises a switch.
17. The method according to claim 11 , wherein the strip-type identifier comprises a circuit loop.
18. The method according to claim 1 , wherein the biosensor comprises an identifier indicating a universal calibration code.Cited by (0)
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